📂 Diseases
Bardet-Biedl syndrome 15 — Definition
Bardet-Biedl sendromu tip 15 / Bardet-Biedl syndrome 15
Bardet-Biedl syndrome type 15 is a rare genetic disease, showing autozomal resessive transition. This syndrome is characterized by obesity, retinal dystrophy related vision loss, polymintili (phase finger), kidney anomalies and learning difficulties. Type 15 is welded from mutations in the WDPCP gene and is associated with the eraser dysfunction. The disease requires a multidisciplinary approach because it shows multisystemic retention.
Frequently Asked Questions
❓ What is Bardet-Biedl sendromu tip 15?
Bardet-Biedl sendromu tip 15; bardet-Biedl syndrome type 15 is a rare genetic disease, showing autozomal resessive transition. This syndrome is characterized by obesity, retinal dystrophy related vision loss, polymintili (phase finger), kidney anomalies and learning difficulties. Type 15 is welded from mutations in the WDPCP gene and is associated with the eraser dysfunction. The disease requires a multidisciplinary approach because it shows multisystemic retention.
❓ What is Bardet-Biedl syndrome 15 in Turkish?
The Turkish equivalent of "Bardet-Biedl syndrome 15" is Bardet-Biedl sendromu tip 15.
❓ Which medical field is Bardet-Biedl sendromu tip 15 related to?
This term belongs to the Diseases category.